SNOMED CT

Last uploaded: January 31, 2024
Preferred Name

Aldosterone deficiency

Synonyms

Aldosterone deficiency (disorder)

Hypoaldosteronism

ID

http://purl.bioontology.org/ontology/SNOMEDCT/60086000

Active

1

altLabel

Aldosterone deficiency (disorder)

Hypoaldosteronism

CASE SIGNIFICANCE ID

900000000000020002

900000000000448009

CTV3ID

C1543

cui

C0020595

DEFINITION STATUS ID

900000000000074008

Effective time

20020131

Has finding site

http://purl.bioontology.org/ontology/SNOMEDCT/68594002

notation

60086000

prefLabel

Aldosterone deficiency

Subset member

6011000124106~MAPADVICE~IF FAMILIAL ALDOSTERONE DEFICIENCY CHOOSE E27.49 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~E27.49

447562003~MAPTARGET~E27.4

447562003~MAPRULE~TRUE

6011000124106~MAPPRIORITY~7

6011000124106~MAPPRIORITY~4

6011000124106~MAPRULE~IFA 236464008 | Hyporeninemic hypoaldosteronism |

6011000124106~MAPRULE~IFA 715343000 | Familial aldosterone deficiency (disorder) |

6011000124106~MAPRULE~IFA 47757001 | Corticosterone 18-monooxygenase deficiency |

447562003~MAPADVICE~ALWAYS E27.4

6011000124106~MAPRULE~IFA 1186812001 | Familial hyperreninemic hypoaldosteronism type 2 |

6011000124106~MAPADVICE~IF CORTICOSTERONE 18-MONOOXYGENASE DEFICIENCY CHOOSE E25.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPGROUP~1

6011000124106~MAPRULE~IFA 1217069000 | Familial hyperreninemic hypoaldosteronism type 1B |

6011000124106~MAPPRIORITY~8

6011000124106~MAPRULE~IFA 715343000 | Familial hypoaldosteronism |

6011000124106~MAPADVICE~IF FAMILIAL HYPERRENINEMIC HYPOALDOSTERONISM TYPE 2 CHOOSE E27.49 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

900000000000508004~ACCEPTABILITYID~900000000000549004

6011000124106~MAPADVICE~IF FAMILIAL HYPOALDOSTERONISM CHOOSE E27.49 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 237765003 | Hyperreninemic hypoaldosteronism |

447562003~MAPGROUP~1

6011000124106~MAPTARGET~E25.0

447562003~CORRELATIONID~447561005

6011000124106~MAPCATEGORYID~447637006

900000000000509007~ACCEPTABILITYID~900000000000548007

6011000124106~MAPRULE~IFA 1217075009 | Familial hyperreninemic hypoaldosteronism type 1A |

900000000000508004~ACCEPTABILITYID~900000000000548007

447562003~MAPPRIORITY~1

447562003~MAPCATEGORYID~447637006

6011000124106~MAPADVICE~IF HYPORENINEMIC HYPOALDOSTERONISM CHOOSE E27.49 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~OTHERWISE TRUE

6011000124106~MAPTARGET~E27.40

6011000124106~MAPPRIORITY~5

6011000124106~MAPADVICE~IF FAMILIAL HYPERRENINEMIC HYPOALDOSTERONISM TYPE 1A CHOOSE E27.49 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPCATEGORYID~447639009

6011000124106~MAPRULE~IFA 236464008 | Hyporeninemic hypoaldosteronism (disorder) |

6011000124106~MAPADVICE~ALWAYS E27.40

6011000124106~MAPADVICE~IF HYPERRENINEMIC HYPOALDOSTERONISM CHOOSE E27.49 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPPRIORITY~1

6011000124106~MAPPRIORITY~6

900000000000497000~MAPTARGET~C1543

6011000124106~CORRELATIONID~447561005

6011000124106~MAPRULE~IFA 47757001 | Corticosterone 18-monooxygenase deficiency (disorder) |

6011000124106~MAPPRIORITY~3

900000000000509007~ACCEPTABILITYID~900000000000549004

6011000124106~MAPPRIORITY~2

6011000124106~MAPRULE~IFA 237765003 | Hyperreninemic hypoaldosteronism (disorder) |

6011000124106~MAPADVICE~IF FAMILIAL HYPERRENINEMIC HYPOALDOSTERONISM TYPE 1B CHOOSE E27.49 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

tui

T047

Type ID

900000000000003001

900000000000013009

subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/386584007

http://purl.bioontology.org/ontology/SNOMEDCT/123765007

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